Canonical Allele Identifier: CA2206693467

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764886A= , CM000678.2:g.9764886A=	GRCh38
NC_000016.9:g.9858743A= , CM000678.1:g.9858743A=	GRCh37
NC_000016.8:g.9766244A=	NCBI36
NG_011812.1:g.422869T=
NG_011812.2:g.422869T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2658T= MANE Select	ENSP00000332549.3:p.Asn886=
ENST00000535259.6:c.2187T=	ENSP00000441572.3:p.Asn729=
ENST00000636273.2:n.2251T=
ENST00000674742.1:c.2187T=	ENSP00000502200.1:p.Asn729=
ENST00000675398.1:c.*28T=	ENSP00000502752.1:n.*28T=
ENST00000330684.3:c.2658T=	ENSP00000332549.3:p.Asn886=
ENST00000396573.6:c.2658T=	ENSP00000379818.2:p.Asn886=
ENST00000396575.6:c.2247T=	ENSP00000379820.3:p.Asn749=
ENST00000461292.3:n.2297T=
ENST00000463531.1:n.441T=
ENST00000535259.5:c.2247T=	ENSP00000441572.2:p.Asn749=
ENST00000562109.5:c.2658T=	ENSP00000454998.1:p.Asn886=
NM_000833.4:c.2658T=	NP_000824.1:p.Asn886=
NM_001134407.2:c.2658T=	NP_001127879.1:p.Asn886=
NM_001134408.2:c.2658T=	NP_001127880.1:p.Asn886=
XM_011522456.1:c.2499T=	XP_011520758.1:p.Asn833=
XM_011522457.1:c.2400T=	XP_011520759.1:p.Asn800=
XM_011522458.1:c.2187T=	XP_011520760.1:p.Asn729=
XM_011522459.1:c.2187T=	XP_011520761.1:p.Asn729=
XM_011522460.1:c.2187T=	XP_011520762.1:p.Asn729=
XM_011522461.1:c.2658T=	XP_011520763.1:p.Asn886=
XM_011522458.3:c.2187T=	XP_011520760.1:p.Asn729=
XM_011522461.3:c.2658T=	XP_011520763.1:p.Asn886=
XM_017023172.1:c.2814T=	XP_016878661.1:p.Asn938=
XM_017023173.1:c.2814T=	XP_016878662.1:p.Asn938=
NM_001134407.3:c.2658T= MANE Select	NP_001127879.1:p.Asn886=
NM_000833.5:c.2658T=	NP_000824.1:p.Asn886=